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右美托咪定-瑞芬太尼和丙泊酚-瑞芬太尼镇静方案的有效性及安全性在经皮房间隔缺损封堵术中的比较摘要:
目的:比较右美托咪定-瑞芬太尼和丙泊酚-瑞芬太尼镇静方案在经皮房间隔缺损封堵术中的有效性和安全性。
方法:选取2019年1月至2021年4月在本院行经皮房间隔缺损封堵术的患者162例,随机分为右美托咪定-瑞芬太尼组(82例)和丙泊酚-瑞芬太尼组(80例)。记录术前基本信息、监测指标、术中镇静质量、并发症及手术相关指标,并对比两组。
结果:两组在术前基本信息及监测指标上无统计学差异。右美托咪定-瑞芬太尼组和丙泊酚-瑞芬太尼组的T1%、T2%、T3%、T4%、T5%均达到了良好至优秀。右美托咪定-瑞芬太尼组较丙泊酚-瑞芬太尼组在血流动力学指标的变化较小,差异有统计学意义(P<0.05)。术中无严重并发症发生,两组患者的手术时间、导管成功率、成功封堵率、手术效果等指标均无明显差异。
结论:右美托咪定-瑞芬太尼和丙泊酚-瑞芬太尼在经皮房间隔缺损封堵术中均有效、安全,但右美托咪定-瑞芬太尼组在血流动力学方面的变化小于丙泊酚-瑞芬太尼组。因此,在经皮房间隔缺损封堵术中可以采用两种方案。
关键词:右美托咪定;丙泊酚;瑞芬太尼;经皮房间隔缺损封堵术;镇静方案;血流动力学指标
Abstract:
Objective:Tocomparetheeffectivenessandsafetyofdexmedetomidine-remifentanilandpropofol-remifentanilsedationschemesinpercutaneousatrialseptaldefectclosure(ASDC).
Methods:Atotalof162patientswithpercutaneousASDCfromJanuary2019toApril2021weredividedintodexmedetomidine-remifentanilgroup(82cases)andpropofol-remifentanilgroup(80cases).Thebasicinformation,monitoringindicators,sedationqualityduringsurgery,complicationsandsurgicalrelatedindicatorswererecordedandcomparedbetweenthetwogroups.
Results:Therewasnostatisticaldifferenceinbaselineinformationandmonitoringindicatorsbetweenthetwogroups.BothT1%,T2%,T3%,T4%,andT5%ofdexmedetomidine-remifentanilgroupandpropofol-remifentanilgroupachievedgoodtoexcellent.Thechangesinhemodynamicindicatorsinthedexmedetomidine-remifentanilgroupweresmallerthanthoseinthepropofol-remifentanilgroup,andthedifferencewasstatisticallysignificant(P<0.05).Therewerenoseriouscomplicationsduringtheoperation,andtherewasnosignificantdifferenceinoperationtime,successrateofguidewire,successrateofclosureandsurgicaleffectbetweenthetwogroups.
Conclusion:Bothdexmedetomidine-remifentanilandpropofol-remifentanilsedationschemesareeffectiveandsafeinpercutaneousASDC,butthechangesinhemodynamicindicatorsindexmedetomidine-remifentanilgroupweresmallerthanthoseinpropofol-remifentanilgroup,sobothschemescanbeusedinpercutaneousASDC.
Keywords:Dexmedetomidine;Propofol;Remifentanil;Percutaneousatrialseptaldefectclosure;Sedationscheme;HemodynamicindicatorInrecentyears,percutaneousatrialseptaldefectclosurehasbecomeapopularalternativetosurgicalclosureinselectedpatients.Sinceconscioussedationisusuallyusedduringtheprocedure,choosinganappropriatesedationschemeiscrucial.Inthisstudy,wecomparedtheefficacyandsafetyoftwocommonlyusedsedationschemes:dexmedetomidine-remifentanilandpropofol-remifentanil.
OurresultsshowedthatbothsedationschemeswereeffectiveinachievingadequatesedationandanalgesiaduringpercutaneousASDC.Patientsinbothgroupshadnosignificantdifferencesintermsofsedationlevel,analgesia,orproceduralsuccessrate.However,thechangesinhemodynamicindicatorsinthedexmedetomidine-remifentanilgroupweresmallerthanthoseinthepropofol-remifentanilgroup.Thissuggeststhatdexmedetomidinemayprovidebetterhemodynamicstabilityduringtheprocedure.
Additionally,wefoundthattheincidenceofadverseeventswaslowinbothgroups,withnoseriouscomplicationsreported.ThisindicatesthatbothsedationschemesaresafeforuseduringpercutaneousASDC.
Inconclusion,ourstudysuggeststhatbothdexmedetomidine-remifentanilandpropofol-remifentanilsedationschemesareeffectiveandsafeforuseduringpercutaneousASDC.However,thedexmedetomidine-remifentanilschememayofferbetterhemodynamicstability.Overall,thechoiceofsedationschemeshouldbebasedonpatientfactors,proceduralconsiderations,andthepreferencesoftheanesthesiateamOnelimitationofourstudyisthesmallsamplesize,whichmaylimitthegeneralizabilityofourresults.Additionally,ourstudyfocusedonlyontheacuteeffectsofsedationduringpercutaneousASDC,andfurtherstudiesareneededtoevaluatethelong-termoutcomesofdifferentsedationschemes.
Anotherareaforfutureresearchisthecomparisonofdifferentdosesofsedatives,aswellastheuseofadjunctiveagentssuchasketamineormidazolam.Additionally,theroleofregionalanesthesiatechniquessuchasthoracicepiduralorparavertebralblocksinreducingtheneedforsedationduringpercutaneousASDCshouldalsobeexplored.
Furthermore,theuseofsedationduringpercutaneousASDCmustalwaysbebalancedagainstthepotentialrisks,includingrespiratorydepression,hemodynamicinstability,andadversedrugreactions.Therefore,carefulpatientselection,monitoring,andappropriatedosingareessentialtoensuresafeandeffectivesedationduringtheseprocedures.
Inconclusion,sedationwitheitherdexmedetomidine-remifentanilorpropofol-remifentanilappearstobesafeandeffectiveforpercutaneousASDC.Whiledexmedetomidine-remifentanilmayprovidebetterhemodynamicstability,thechoiceofsedationshouldbebasedonindividualpatientfactorsandproceduralconsiderations.FurtherresearchisneededtooptimizesedationstrategiesforpercutaneousASDCandtobetterunderstandthelong-termoutcomesandpotentialrisksassociatedwithsedationinthispopulationInadditiontosedationstrategies,thereareotherfactorsthatcanimpactthesafetyandeffectivenessofpercutaneousASDC.Theseincludetheexperienceandskilloftheoperator,thetypeandsizeoftheclosuredeviceused,andthepresenceofcomorbiditiessuchaspulmonaryhypertensionorsevereobesity.Appropriatepatientselectionisalsocritical,assomepatientsmaynotbesuitablecandidatesforpercutaneousASDCduetoanatomicalorhemodynamicfactors.
OneareaofongoingresearchistheuseofadvancedimagingtechniquestoguidepercutaneousASDCprocedures.Thisincludestheuseofthree-dimensionalechocardiography,whichcanprovidemoredetailedinformationaboutthesizeandshapeofthedefectandhelpguidedeviceplacement.Inaddition,theuseofintracardiacechocardiographyorfluoroscopymayalsobebeneficialforguidingdeviceplacement.
Anotherimportantconsiderationisthelong-termoutcomeofpercutaneousASDC.Whilemanypatientsexperiencesignificantimprovementinsymptomsandhemodynamicsfollowingclosure,thereisstillariskofcomplicationssuchasdevicemigration,residualshunting,orthrombusformation.Long-termfollow-upisrecommendedtomonitorforthesecomplicationsandensureoptimalpatientoutcomes.
Inconclusion,percutaneousclosureofASDisasafeandeffectivealternativetosurgicalrepairinselectpatients.Appropriatepatientse
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